Sansone Valeria A, Burge James, McDermott Michael P, Smith Patty C, Herr Barbara, Tawil Rabi, Pandya Shree, Kissel John, Ciafaloni Emma, Shieh Perry, Ralph Jeffrey W, Amato Antony, Cannon Steve C, Trivedi Jaya, Barohn Richard, Crum Brian, Mitsumoto Hiroshi, Pestronk Alan, Meola Giovanni, Conwit Robin, Hanna Michael G, Griggs Robert C
From NEMO Clinical Center (V.A.S.) and IRCCS Policlinico San Donato (G.M.), University of Milan, Italy; MRC Centre for Neuromuscular Diseases (J.B., M.G.H.), UCL Institute of Neurology, Queen Square, London, UK; University of Rochester (M.P.M., P.C.S., B.H., R.T., S.P., E.C., R.C.G.), NY; Ohio State University (J.K.), Columbus; UCLA Medical Center (P.S.), Los Angeles, CA; University of California San Francisco School of Medicine (J.W.R.); Brigham and Women's Hospital (A.A.), Boston, MA; UT Southwestern Medical Center (S.C.C., J.T.), Dallas, TX; University of Kansas Medical Center (R.B.), Kansas City; Mayo Clinic (B.C.), Rochester MN; Columbia University (H.M.), New York, NY; Washington University (A.P.), St. Louis, MO; and the Office of Clinical Research (R.C.), NINDS, Bethesda, MD.
Neurology. 2016 Apr 12;86(15):1408-1416. doi: 10.1212/WNL.0000000000002416. Epub 2016 Feb 10.
To determine the short-term and long-term effects of dichlorphenamide (DCP) on attack frequency and quality of life in hyperkalemic (HYP) and hypokalemic (HOP) periodic paralysis.
Two multicenter randomized, double-blind, placebo-controlled trials lasted 9 weeks (Class I evidence), followed by a 1-year extension phase in which all participants received DCP. Forty-four HOP and 21 HYP participants participated. The primary outcome variable was the average number of attacks per week over the final 8 weeks of the double-blind phase.
The median attack rate was lower in HOP participants on DCP than in participants on placebo (0.3 vs 2.4, p = 0.02). The 9-week mean change in the Physical Component Summary score of the Short Form-36 was also better in HOP participants receiving DCP (treatment effect = 7.29 points, 95% confidence interval 2.26 to 12.32, p = 0.006). The median attack rate was also lower in HYP participants on DCP (0.9 vs 4.8) than in participants on placebo, but the difference in median attack rate was not significant (p = 0.10). There were no significant effects of DCP on muscle strength or muscle mass in either trial. The most common adverse events in both trials were paresthesia (47% DCP vs 14% placebo, both trials combined) and confusion (19% DCP vs 7% placebo, both trials combined).
DCP is effective in reducing the attack frequency, is safe, and improves quality of life in HOP periodic paralysis.
These studies provide Class I evidence that DCP significantly reduces attack frequency in HOP but lacked the precision to support either efficacy or lack of efficacy of DCP in HYP.
确定二氯苯磺胺(DCP)对高钾型(HYP)和低钾型(HOP)周期性麻痹发作频率及生活质量的短期和长期影响。
两项多中心随机、双盲、安慰剂对照试验持续9周(I级证据),随后是为期1年的延长期,在此期间所有参与者均接受DCP治疗。44名HOP参与者和21名HYP参与者参与了试验。主要结局变量是双盲期最后8周每周的平均发作次数。
服用DCP的HOP参与者的发作率中位数低于服用安慰剂的参与者(0.3对2.4,p = 0.02)。接受DCP治疗的HOP参与者在简短健康调查问卷-36的身体成分总结评分方面,9周的平均变化也更好(治疗效果=7.29分,95%置信区间2.26至12.32,p = 0.006)。服用DCP的HYP参与者的发作率中位数(0.9对4.8)也低于服用安慰剂的参与者,但发作率中位数的差异不显著(p = 0.10)。在两项试验中,DCP对肌肉力量或肌肉量均无显著影响。两项试验中最常见的不良事件是感觉异常(DCP组47%对安慰剂组14%,两项试验合并)和意识模糊(DCP组19%对安慰剂组7%,两项试验合并)。
DCP可有效降低HOP周期性麻痹的发作频率,安全且可改善生活质量。
这些研究提供了I级证据,表明DCP可显著降低HOP的发作频率,但缺乏精确性来支持DCP在HYP中的疗效或无效性。